Phosphatidylcholine produced in rat synaptosomes by N-methylation is enriched in polyunsaturated fatty acids.

AUTOR(ES)

Tacconi, M

RESUMO

Rat brain synaptosomes contain an enzyme, phosphatidylethanolamine N-methyltransferase (EC 2.1.1.17), that catalyzes the methylation of phosphatidylethanolamine to form its mono-, di-, and trimethyl (phosphatidylcholine) derivatives. Synaptosomal phosphatidylethanolamine is much richer in polyunsaturated fatty acids (43.4%) than is synaptosomal phosphatidylcholine (4.6%). It thus seemed possible that the phosphatidylcholine derived via the N-methylation of phosphatidylethanolamine might also be especially enriched in polyunsaturated fatty acids. To test this hypothesis, we examined the incorporation of [3H]methyl groups into various molecular species of phosphatidylcholine, by incubating rat synaptosomes for 10, 30, or 90 min in a medium containing S-adenosyl[methyl-3H]methionine. Phosphatidylcholine was extracted and separated from other lipids by TLC, after which its molecular species were isolated by argentation TLC (which distinguishes among the phospholipid molecules by the degree of unsaturation of their fatty acid moieties.) We found that approximately 65% of the [3H]methyl incorporated into phosphatidylcholine during the incubation period was present in the fraction associated with pentaene or hexaene fatty acids; an additional 30% was present in the tetraene fraction, while the remaining phosphatidylcholine radioactivity was distributed between the dienes and monoenes. Similar distributions were observed among synaptosomes incubated for 10 or 30 min; however, after 90 min the phosphatidyl[3H]choline contained proportionately less of the tetraenes. These observations indicate that neuronal phosphatidylcholine molecules formed via N-methylation are especially richer in polyunsaturated fatty acids, and they raise the possibility that these molecules constitute a distinct pool with particular physiologic functions.

Documentos Relacionados

• Alterations in phospholipid N-methylation of cardiac subcellular membranes due to experimentally induced diabetes in rats.
• Modulation of human hepatocyte acute phase protein production in vitro by n-3 and n-6 polyunsaturated fatty acids.
• The role of n-3 polyunsaturated fatty acids in brain: Modulation of rat brain gene expression by dietary n-3 fatty acids
• A single bifunctional enzyme, PilD, catalyzes cleavage and N-methylation of proteins belonging to the type IV pilin family.
• External blockade of the major cardiac delayed-rectifier K+ channel (Kv1.5) by polyunsaturated fatty acids.